google-site-verification=cXrcMGa94PjI5BEhkIFIyc9eZiIwZzNJc4mTXSXtGRM Black, 40, previous stillbirth. Mom’s death from sepsis led dad to push for personalized pregnancy care - 360WISE MEDIA
Connect with us

Lifestyle

Black, 40, previous stillbirth. Mom’s death from sepsis led dad to push for personalized pregnancy care

Published

on

Black mother health

Clayton Anderson said that despite a previous stillbirth, his late wife Krystal Anderson received the identical level of preventive care because the 23-year-old, who could be very healthy.

Former Kansas City Chiefs cheerleader Krystal “Krissy” Anderson and her husband Clayton Anderson felt they finally had one other likelihood to expand their family once they came upon last November that she was pregnant again. Her pregnancy with baby James resulted in stillbirth. But on the age of 40, Krystal became pregnant again.

Clayton said ABC news he saw their second likelihood at parenthood as a “little sign” from James. Although the couple believed he was sending them a hopeful message, they’d doubts. Krystal was black. She was older. She had lost a toddler before.

Only one in all these aspects was particularly dangerous, however the Andersons had to take care of the dreaded trio. Clayton told the ABC they asked for high-risk care from the beginning. But doctors told the couple they might have to wait until Krystal was three and a half months pregnant, he said, because “you can’t start a plan with maternal-fetal medicine or high-risk obstetricians until the 14th week.” “

Clayton Anderson is speaking out against the maternal health care system following the death of his wife, Krystal Anderson, who appears in a framed photo behind him. (Photo: Screenshot/YouTube.com/KSHB 41 News)

“Every pregnancy is high risk, especially if you are a woman of color or older,” Clayton said, “and women should be treated as such from the beginning.”

Krystal died on March 20, four weeks before receiving the specialized care she and her husband wanted. Unfortunately, Krystal’s result is the same for many black mothers, who are at least three times more likely to die from pregnancy-related complications compared to white women. Charlotte Willow, the Andersons’ daughter, died four days before her mother. And like her, Charlotte has become another tragic data point that shows that black babies – even those born to wealthy mothers – die at higher rates than those born to poor white mothers.

The Black community knows well-known and affluent Black mothers who must fight alone for proper care during pregnancy and after childbirth. Tennis champion Serena Williams had to defend herself after several blood clots formed in her lungs following the 2017 birth by caesarean section of her first daughter, Alexis Olympia. Four years earlier, actress Kyla Pratt had an experience with a dismissive caregiver who initially ignored her concerns about contractions while she was giving birth to her second child.

Clayton Anderson is now speaking out against “one size suits all” prenatal care in honor of his late wife, who at the age of 40 advanced maternal age and are automatically at greater risk of pregnancy complications.

In December, a month after finding out she was pregnant, Krystal feared she might miscarry. She underwent cerclage surgery at 16 weeks to ensure her viability for the rest of her pregnancy. The next doctor’s visit was scheduled for week 20.

“Expecting someone who has suffered a loss to have 4 weeks between visits to their caregivers… It’s the identical protocol that is used for a 23-year-old who could be very healthy,” Clayton said. “It can’t be a one-size-fits-all solution.”

After complications in March, doctors planned to place his wife in a specialized hospital unit where she would be able to give birth successfully if she lived to 22 weeks. At her 20-week appointment, Clayton said doctors started prescribing her a semi-recumbent position for two weeks to help her get to that point.

On Saturday, March 16, still in her 20th week, Krystal began experiencing back pain, which her obstetrician suggested could be a sign of cramps and dehydration. Clayton stated that after conducting tests, doctors discovered amniotic fluid and ultimately stopped detecting the fetal heartbeat.

Krystal underwent surgery the next morning and was back on a ventilator and dialysis machine, experiencing kidney, liver and lung failure. She died within a few days.

The Mayonnaise clinic defines sepsis as “a serious condition in which the body responds inappropriately to an infection.” According to Centers for Disease Control and PreventionSepsis affects 1.7 million adults in the U.S. each year, causing nearly 270,000 deaths annually.

Medical Journal Healthcarepublished in the National Library of Medicine states that in black and Hispanic communities, the incidence and mortality from sepsis are higher than in the white population. While disparities are often blamed on systemic bias against minority groups, the journal noted that “a growing body of literature indicates that patient, community and hospital aspects are the reason for racial disparities.”

According to ABC News, AdventHealth Shawnee Mission declined to provide details about Krystal Anderson’s care due to the Health Insurance Portability and Accountability Act (HIPAA), but the hospital sent its condolences to the family.

“Our hearts ache at this tragic situation,” they wrote in a statement, ABC reported. “Together with the independent providers who provide care at our facilities, we strive to provide each patient with the best possible care based on their specific needs and circumstances. Our prayers and support go out to family members and loved ones experiencing the devastating loss of a precious life.”

!function(){var g=window;g.googletag=g.googletag||{},g.googletag.cmd=g.googletag.cmd||(),g.googletag.cmd.push(function(){ g.googletag.pubads().setTargeting(“has-recommended-video”,”true”)})}();var _bp=_bp||();_bp.push({“div”:”Brid_21904″, “obj”:{“id”:”41122″,”width”:”1280″,”height”:”720″,”stickyDirection”:”below”,”playlist”:”21904″,”slide_inposition”:” .widget_tpd_ad_widget_sticky”}});

Featured Stories

Post Black, 40, previous stillbirth. Mom’s death from sepsis led dad to push for personalized pregnancy care. First appeared on TheGrio.

This article was originally published on : thegrio.com
Continue Reading
Advertisement
Click to comment

Leave a Reply

Your email address will not be published. Required fields are marked *

Lifestyle

Opal Lee, “Juneteenth’s Grandma,” will receive her eighth honorary doctorate for her unwavering commitment to civil rights

Published

on

By

Opal Lee will soon receive her eighth honorary doctorate in recognition of her legacy of activism and unwavering commitment to civil rights.

According to People MagazineSouthern Methodist University will present the 97-year-old “Grandma of Juneteenth” with an honorary Doctor of Philosophy degree at a commencement ceremony on May 11.

“For Ms. Lee to join us at the commencement and share her work during the symposium is a signal of honor for our university” – SMU President R. Gerald Turner – wrote within the statement. “Her life’s work is most deserving of this recognition, and our students will be inspired by her.”

Opal Lee (left) claps throughout the ceremony before constructing the primary wall of her latest home on land her family purchased in Fort Worth, Texas, last month. (Photo by Amanda McCoy/Star-Telegram via AP)

In 2016, Lee, 89, made a symbolic 2,500-kilometer walk from her home in Fort Worth, Texas, to Washington, D.C., to urge Congress and then-President Barack Obama’s administration to declare June 11 a federal holiday honoring the tip of slavery. after the civil war. She stood nearby when President Joe Biden formally signed the bill into law five years in a while June 17, 2021.

“I must tell you that I have only been president for a few months, but I think this will go down as one of the greatest honors that I will experience as president – not because I did it, but because you did it, Democrats and Republicans.” Biden told her on the time, People magazine reported. “It’s a huge, huge honor.”

Lee’s dream of rebuilding her childhood home, destroyed by a racist mob in 1939, got here true in December when she purchased the land where the home once stood. After years of trying to buy the land, Lee discovered that Trinity Habitat for Humanity had purchased it. The organization’s CEO, Gage Yager, informed her that a plot of land in Fort Worth was available, Washington Post. she got here forward, sold it to her for just $10, and offered to construct her a house. Last month, she helped construct its first wall.

Featured Stories

According to SMU, Lee will achieve one other of her goals with the planned opening of the $70 million, 50,000-square-foot National Juneteenth Museum on south Fort Worth, where she operated her own modest Juneteenth museum.

The latest constructing will function a museum, cultural center and business incubator, and will be home to a mixed-income housing community. Lee is the museum’s honorary chairwoman and, together with her granddaughter, is a current board member.

Among the notable nods, as well as to seven other Ph.D.s, the Dallas Morning News editorial board named Lee its 2021 Texan of the Year, and he or she is nominated for a Nobel Peace Prize in 2022. In 2023, she became the second African-American woman, after the late Republican Barbara Jordan, to be honored with a portrait in chamber of the Texas State Senate, SMU reports.


This article was originally published on : thegrio.com
Continue Reading

Lifestyle

Meghan Markle and Prince Harry will soon go to Nigeria

Published

on

By

According to reports, the subsequent stop on the Duke and Duchess of Sussex’s world tour will be Nigeria.

Meghan Markle and Prince Harry will arrive within the country in May on the invitation of the Nigerian Chief of Defense Staff. During their visit to the African country, the couple will take part in native cultural events and meet with various service members.

The invitation to visit was reportedly initiated by Harry Invictus games, a sporting event he designed after discovering how “sports can help wounded servicemen and women recover—physically, mentally and socially.” Considered one in all the prince’s few ties with the royal family, 500 athletes from 21 countries took part last yr in Germany, where Nigeria was supported by the duchess herself. Although the 2025 Invictus Games are scheduled to be held in Canada, Nigeria has expressed interest in hosting a future event.

“The visit is intended to strengthen Nigeria’s position at the match and enable it to host the event in later years,” Brigadier General Tukur Gusau, Nigeria’s acting director of defense information, said in an announcement, according to People Magazine.

Featured Stories

During last yr’s event, the couple took a specific liking to the Nigerian team. In 2022, after learning she was 43% Nigerian during a genealogy test, Markle revealed her newfound heritage on her award-winning podcast, Archetypes.

“I’m going to start digging into all this because everyone I’ve told, especially Nigerian women, is like, ‘What!’” she said on the show.

In light of this revelation, Markle and her husband reportedly frolicked with the Nigerian national team on the 2023 Invictus Games, where the Duchess of Sussex was given a brand new nickname. Like her royal title, her Nigerian name “Amira Ngozi Lolo” has a royal meaning, with “Amira” meaning warrior princess of legend, “Ngozi” meaning blessed one, and Lolo meaning “royal wife”.

“I’m not saying we’re playing favorites in our house, but since my wife discovered she’s of Nigerian descent, it’s probably going to be a little more competitive this year,” Prince Harry said in his 2023 commencement speech, teasing that one in all them a team that the duchess will support.



This article was originally published on : thegrio.com
Continue Reading

Lifestyle

For black women in the U.S., the odds of surviving breast cancer need to change

Published

on

By

Dr. Aida Habtezion

The Seventies were marked by the “second wave” of feminism the starting of the breast cancer awareness movement, in which several distinguished public figures drew attention to the need for education, research and support for this disease. Since then, great strides have been made in stopping, detecting and treating breast cancer, and significantly fewer women are actually dying from the disease. However, this progress has not benefited everyone equally; Black women are 40% more likely to die from breast cancer compared to white women. The difference amongst younger women is much more stark: Black women under the age of 50 are twice as likely to die from breast cancer as white women of the same age.

As a physician and scientist – and as an individual of African descent – ​​I’m acutely aware of the devastating impact breast cancer has on our community. In my greater than twenty years of clinical practice, I’m conversant in the proven fact that the same disease affects people in alternative ways, regardless of race, ethnicity and socioeconomic background.

I’m committed not only to eliminating health disparities, but in addition to higher understanding those that experience them. Who they’re? Where do they live? When they get the life-changing news that they’ve cancer? And when will they find out how to navigate the health care system to receive appropriate and optimal care?

The sad reality is that this Black men and women have lower rates of cancer screening overall. In black women, breast cancer is more likely to be diagnosed in advanced stages, when the disease is more complicated to treat, and it’s triple-negative breast cancer, an aggressive form for which there are fewer treatment options, is twice as likely to be diagnosed. Furthermore, black women have lowest 5-year relative survival rate for every stage of breast cancer at diagnosis. This indicates significant gaps in access to quality care and treatment after diagnosis.

At the heart of these inequalities is a particularly complex history of discrimination, prejudice and distrust in the health care system. This history, combined with the lived experiences of many Black women today, often limit and even prevent them from accessing cancer screening opportunities and in search of care and support after diagnosis. This discrepancy also applies to participation in clinical trials aimed toward developing latest, potentially breakthrough drugs. It is well-known that racial and ethnic minorities proceed to be underrepresented in clinical trials, with recently published data estimating that only roughly 4-7% of participants in cancer clinical trials are Black. Even this small percentage is believed to be an underestimate, on condition that only about one-third of cancer clinical trials take race into consideration. In addition to lack of trust in physicians, aspects contributing to low participation in clinical trials include study design (e.g., lack of diverse recruitment), healthcare skilled bias, recruitment requirements (e.g., exclusion of individuals with other diseases), and barriers to access.

Featured Stories

To achieve true health equity for all and enable Black women to profit from scientific advances in breast cancer screening, diagnosis and care, these disparities should be addressed. Despite the many barriers, I consider that by working together we will find ways to make progress. No one person or organization can address these challenges alone; this can require cooperation and partnership towards a standard mission.

To that end, Pfizer has partnered with the American Cancer Society to start making changes where they’re most urgently needed: in communities which are disproportionately affected by breast and prostate cancer and underserved. By latest “Change the odds” Through this initiative, we are going to raise awareness of free and low-cost screening, increase access to support and patient navigation services, and supply general details about clinical trials.

As a black woman, I understand how necessary it’s to take care of my very own health to get the care I deserve – and I encourage every woman over the age of 40 or younger: If you could have risk aspects, corresponding to family history, seek regular breast screenings towards cancer. However, as a physician and advocate, I do know that the health care community simply needs to do a greater job of advocating for women of color. Every life lost to breast cancer is a life we ​​cannot afford to lose.


As Pfizer’s Chief Medical Officer, Dr. Aida Habtezion leads Pfizer’s global medical and safety organization, chargeable for providing patients, physicians and regulators with details about the protected and appropriate use of Pfizer medicines. He also directs Pfizer’s Translational Medicine Equity Institute, an initiative to achieve health equity. Prior to joining Pfizer, Dr. Habtezion was a practicing physician and scientist at Stanford University School of Medicine, Department of Gastroenterology and Hepatology.


This article was originally published on : thegrio.com
Continue Reading
Advertisement

OUR NEWSLETTER

Subscribe Us To Receive Our Latest News Directly In Your Inbox!

We don’t spam! Read our privacy policy for more info.

Trending